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QualitecFarma®
A Contract Research Organisation (CRO) ready to provide you with complete high-quality, custom solutions in drug development
Discover our solutions for you!
Preclinical Strategies
Tailored nonclinical programs:
  • Management and Monitoring
  • Interpretation of Nonclinical Safety Data
  • Impurities and Excipients Qualifications
  • ERAs and PDEs
Discover our solutions for you!
Clinical Research
Developing the best strategy for all clinical trials with positive results:
  • Phase I
  • Phase II
  • Phase III
  • Phase IV
  • Clinical Pharmacovigilance
Discover our solutions for you!
Pharmacovigilance
  • Clinical Pharmacovigilance
  • Post-marketing Pharmacovigilance
Discover our solutions for you!
Regulatory Affairs
From the early stages to market through well established worldwide Regulatory Intelligence:
  • Full development of dossiers for registration, variations, and renewals
  • Scientific advice and ODDs
  • Expert reports
  • Packaging materials
Discover our solutions for you!
Business Strategies
From business cases to 1st order:
  • Value Dossiers
  • Price and reimbursement
  • SOPs and WIs
  • Tendering services
  • NHS and logistic operators
Discover our solutions for you!
Hello
Preclinical strategies
Clinical research
Pharmacovigilance
Regulatory affairs
Business strategies

About us

Message from the CEO

It is my pleasure to welcome you to QualitecFarma®’s website, the reference company based in Spain for pharmaceutical services to the industry.

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Why choose us

With deep knowledge and high expertise in clinical research, our qualifications allow us to adapt to our clients’ operational and strategic needs, ensuring their success and research promotion.
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Our solutions

Clinical Operations

QualitecFarma® clients have access to fast, flexible, and full services led by our Clinical Operations unit with over 20 years of experience.
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Quality Assurance

Thanks to a well-structured Quality Department, we have a highly qualified GCP system in place, granting the implementation of quality assurance in all our studies.
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Pharmacovigilance

Maintaining trial integrity and post-marketing surveillance are tasks entrusted to our human pharmacovigilance experts. Our responsibilities also extend to providing support in veterinary pharmacovigilance.
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Regulatory Affairs

Time-saving and cost effectiveness from the early stages to market through reliable and well established worldwide Regulatory Intelligence, with an in-depth collaboration with experts in our clinical research team.
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Market Access

Decision-making processes throughout the search for business opportunities starting from dossier development and up to strategic planning of international registration procedures till the launch of the medicine on the market.
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